Adenosine generation catalyzed by CD39 and CD73 expressed on regulatory T cells mediates immune suppression

Author:

Deaglio Silvia1,Dwyer Karen M.1,Gao Wenda1,Friedman David1,Usheva Anny1,Erat Anna1,Chen Jiang-Fan2,Enjyoji Keiichii1,Linden Joel3,Oukka Mohamed4,Kuchroo Vijay K.4,Strom Terry B.15,Robson Simon C.1

Affiliation:

1. Department of Medicine

2. Boston University Medical Center, Boston, MA 02118

3. Department of Medicine, University of Virginia, Charlottesville, VA 22908

4. Department of Neurology, Center for Neurological Diseases, Brigham and Women's Hospital, Boston, MA 02115

5. Department of Surgery, Harvard Medical School, Transplantation Research Center, Beth Israel Deaconess Medical Center, Boston, MA 02215

Abstract

The study of T regulatory cells (T reg cells) has been limited by the lack of specific surface markers and an inability to define mechanisms of suppression. We show that the expression of CD39/ENTPD1 in concert with CD73/ecto-5′-nucleotidase distinguishes CD4+/CD25+/Foxp3+ T reg cells from other T cells. These ectoenzymes generate pericellular adenosine from extracellular nucleotides. The coordinated expression of CD39/CD73 on T reg cells and the adenosine A2A receptor on activated T effector cells generates immunosuppressive loops, indicating roles in the inhibitory function of T reg cells. Consequently, T reg cells from Cd39-null mice show impaired suppressive properties in vitro and fail to block allograft rejection in vivo. We conclude that CD39 and CD73 are surface markers of T reg cells that impart a specific biochemical signature characterized by adenosine generation that has functional relevance for cellular immunoregulation.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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